guise tinted drops
Generic: zinc oxide
Labeler: donis men llcDrug Facts
Product Profile
Brand Name
guise tinted drops
Generic Name
zinc oxide
Labeler
donis men llc
Dosage Form
LOTION
Routes
Active Ingredients
zinc oxide 132 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
83827-1208
Product ID
83827-1208_3f039049-5006-2888-e063-6294a90a5150
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2025-02-11
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
838271208
Hyphenated Format
83827-1208
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
guise tinted drops (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 132 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (83827-1208-2) / 30 mL in 1 BOTTLE (83827-1208-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3f039049-5006-2888-e063-6294a90a5150", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["3f039049-5004-2888-e063-6294a90a5150"], "manufacturer_name": ["Donis Men LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (83827-1208-2) / 30 mL in 1 BOTTLE (83827-1208-1)", "package_ndc": "83827-1208-2", "marketing_start_date": "20250211"}], "brand_name": "Guise Tinted Drops", "product_id": "83827-1208_3f039049-5006-2888-e063-6294a90a5150", "dosage_form": "LOTION", "product_ndc": "83827-1208", "generic_name": "Zinc Oxide", "labeler_name": "Donis Men LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guise Tinted Drops", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "132 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250211", "listing_expiration_date": "20261231"}